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streptococcus mutans     
相关语句
  变形链球菌
    Influence of Tea Catechin on the Synthesis of Extracellular Glucan and the Adherence of Streptococcus Mutans Bacteria
    茶儿茶素影响细胞外多糖合成和变形链球菌附着的研究
短句来源
    Polymerase chain reaction amplification of the spaP gene of streptococcus mutans antigen Ⅰ/Ⅱ
    变形链球菌表面抗原Ⅰ/Ⅱ基因片段的聚合酶链反应扩增
短句来源
    Southern hybridization analysis of the amplification from streptococcus mutans surface antigen Ⅰ/Ⅱ
    变形链球菌表面抗原Ⅰ/Ⅱ基因体外扩增片段的Southern杂交分析
短句来源
    The Immune Response in Rats Immunized Systemically by the Surface Protein Antigen P1 from Streptococcus Mutans Conjugated with Procholeragenoid
    大鼠对变形链球菌表面蛋白P1与前霍乱原类毒素偶联物的免疫应答研究
短句来源
    Effect of surfactant Zonyl FSC on the mutan production of streptococcus mutans
    表面活性剂Zonyl FSC对变形链球菌合成变聚糖的影响
短句来源
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  变异链球菌
    Construction of glucan-binding protein D gene inactivation mutant of Streptococcus mutans
    变异链球菌葡聚糖结合蛋白D基因失活菌株的构建和鉴定
短句来源
    Preliminary Studies on Screening Interaction Proteins from Agkistrodon acutus Venom by Specific Absorption of Streptococcus mutans
    利用变异链球菌特异性吸附筛选蕲蛇毒作用蛋白的初步探讨
短句来源
  变链球菌
    Bacteriolytic enzyme R1 was purified to electrophoretic homogeneity with the recovery of 6.89% activity by ammonium sulfate precipitation, CM-Sephadex C-50, CM-Sepharose Fast Flow and Sephadex G-75 chromatography from the culture supernatant of Streptomyces griseus RX-17. The molecular weight and PI of R1 were 16.8kD and 9.10. The optimal temperature and pH for R1 against Streptococcus mutans Ingbritt were 70℃ and 6.6, respectively.
    通过硫酸铵分级沉淀 ,CM SephadexC 5 0、CM SepharoseFastFlow离子交换层析及Seph adexG 75凝胶过滤层析 ,从灰色链霉菌 (Streptomycesgriseus)RX 1 7的发酵上清液中得到了电泳纯的溶菌酶R1 ,回收率 6 89%。 测得该酶分子量和等电点分别为 1 6 8kD和 9 1 0 ,作用于变链球菌 (Streptococcusmutans)Ingbritt的最适温度和pH分别为 70℃和 6 6。
短句来源
    The enzyme had a broad bacteriolytic spectrum against many G +、G - bacteria which were resistant to egg-white lysozyme. Especially high activity was shown on Streptococcus mutans, Staphylococcus aureus and Lactobaillus .
    R1酶溶菌谱广泛 ,对多种卵清溶菌酶不能作用的G+、G 细菌均有溶解能力 ,对变链球菌、金黄色葡萄球菌 (Staphylococcusaureus)、乳杆菌(Lactobacillus)等则呈现高活性。
短句来源
    Actinomycetes RX-17 with high bacteriolytic activity was isolated from soils by the double layer plates containing intact cells of Streptococcus mutans, and it has been classified into Streptomyces flavus.
    在添加变链球菌 (Streptococcusmutans)菌体的双层平板上 ,筛选到一株产溶菌酶能力较高的放线菌RX 17,将其初步归为链霉菌黄色类群 .
短句来源
  变性链球菌
    Protein Preparation, Crystallization and Preliminary X-ray Crystallographic Analysis of Smu_195c From Caries Pathogen Streptococcus mutans
    龋齿致病菌变性链球菌蛋白Smu_195c的制备、结晶及初级晶体学分析(英文)
短句来源

 

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      streptococcus mutans
    Dentin samples obtained from bovine incisors were immersed in sterile broth supplemented by Lactobacillus acidophillus 108 colony formation units (CFU) and Streptococcus mutans 108 CFU.
          
    Uptake of saccharin and related intense sweeteners by Streptococcus mutans NCTC 10449
          
    The uptake of saccharin into Streptococcus mutans led to a 30 to 40-fold higher concentration of this intense sweetener within cells than in the incubation medium.
          
    W?hrend der dreiw?chigen Zeitspanne vor dem Bekleben reduzierten sich in beiden Gruppen die Durchschnittswerte des VPI, GBI und des Gehaltes an Streptococcus mutans in der Plaque.
          
    DNA vaccine plasmids were constructed that encoded two highly-conservative regions of a surface protein, PAc, from the human major cariogenic bacterium,Streptococcus mutans.
          
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    Aim: Amplification of Streptococcus mutans antigen Ⅰ/Ⅱ. Methods: According to the sequence of the structural gene spaP, we designed and synthesized a couple of oligodeoxynucleotide primers. Using these primers, polymerase chain reaction was employed. Results: Specific amplification of DNA extracted from strains of 13 Streptocooccus mutans and 23 oral permanent bacteria. Six strains of Streptococcus mutans and partial oral permanent bacteria existing 1017bp DNA fragments. Conclusions: These...

    Aim: Amplification of Streptococcus mutans antigen Ⅰ/Ⅱ. Methods: According to the sequence of the structural gene spaP, we designed and synthesized a couple of oligodeoxynucleotide primers. Using these primers, polymerase chain reaction was employed. Results: Specific amplification of DNA extracted from strains of 13 Streptocooccus mutans and 23 oral permanent bacteria. Six strains of Streptococcus mutans and partial oral permanent bacteria existing 1017bp DNA fragments. Conclusions: These findings can serve as a guidance for oral microecology research.

    目的:扩增变形链球菌表面抗原Ⅰ/Ⅱ基因片段,并作特异性鉴定。方法:根据其结构基因spaP序列设计1对寡核苷酸引物,采用聚合酶链反应(PCR)方法扩增了其中长1017bp的片段。结果:所设计的引物能从6株变形链球菌标准株和部分口腔常居菌中扩增出大小一致的DNA片段,结论:该基因部分序列广泛存在于变形链球菌和部分口腔常居菌,为研究口腔细菌的微生态关系提供了新的信息

    Aim:Further study of the specification of amplified products. Methods: The amplified DNA fragments of 1 017bp from streptococcus mutans NG 8 strain were purified and with which to prepare labelled DNA probe using-PdCTP by a random priming procedure. Then Southern hybridization was undertaken using the labelled probe with the amplified fragments of 13 strains was represented strongly hybridized with the labeled probe. Results: There were 6 strains with hybridization. Conclusions: The amplified products...

    Aim:Further study of the specification of amplified products. Methods: The amplified DNA fragments of 1 017bp from streptococcus mutans NG 8 strain were purified and with which to prepare labelled DNA probe using-PdCTP by a random priming procedure. Then Southern hybridization was undertaken using the labelled probe with the amplified fragments of 13 strains was represented strongly hybridized with the labeled probe. Results: There were 6 strains with hybridization. Conclusions: The amplified products by PCR were specific from spaP DNAs.

    目的:研究扩增产物的特异性。方法:将变链菌NG8spaP基因1017bp扩增产物,采用随机引物标记法,使用α-32PdCTP标记成DNA探针,与13株变链菌相应的扩增产物进行Southern杂交。结果:6株有强杂交信号,与PCR结果一致,结论:说明扩增产物是特异的

    Aim: To study the mechanism of streptococcus mutans adhesion. Methods: Using 1 017bp amplified DNA fragments from NG 8 as template, generation of single-stranded DNA by the polymerase chain reaction and its application to direct sequencing of the gene: spaP. Results: Similar to those described previously by Okahashi et al (1989). Conclusions: This group may provide new message for the mechanism of streptococcus mutans adhesion and these research of dental plaque.

    目的:探讨变形链球菌粘附机制。方法:以变形链球菌NG8基因1017bp扩增产物作模板,采用不对称聚合酶链反应(PCR)法扩增单链DNA片段进行序列测定分析。结果:与文献报道的序列一致。结论:为进一步研究菌斑和变形链球菌粘附机制提供了重要信息

     
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